Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-Control Study and a Meta-Analysis

Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-Control Study and a Meta-Analysis


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دانشگاه علوم پزشکی تبریز
دانشگاه علوم پزشکی تبریز

نویسندگان: یونس آفتابی

کلمات کلیدی: Breast cancer . CCND1 gene . Genetic polymorphism . c.870G>A . Meta-analysis

نشریه: 26811 , 3 , 23 , 2017

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله یونس آفتابی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات کاربردی دارویی
کد مقاله 61004
عنوان فارسی مقاله Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-Control Study and a Meta-Analysis
عنوان لاتین مقاله Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-Control Study and a Meta-Analysis
ناشر 6
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ خیر
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت https://link.springer.com/article/10.1007/s12253-016-0165-3

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Cyclin D1 (CCND1) plays an essential role in regulating the progress of the cell cycle from G1 to S phase. There is a common c.870G>A polymorphism in the CCND1 gene. The aim of this study was to investigate the association of CCND1 gene c.870G>A polymorphism with breast cancer risk in a case-control study, which followed by a meta-analysis and an in silico analysis. Three hundred and thirty-five subjects composed of 174 women with breast cancer and 161 healthy controls were included in the case-control study. CCND1 gene c.870G>A genotyping was performed by PCR-RFLP. Meta-analysis was done for 14 studies composed of 7281 cases and 6820 controls. Some bioinformatics tools were applied to investigate the effects of c.870G>A on the mRNA splicing and structure. Our data obtained from casecontrol study revealed that GA genotype (OR: 1.89, 95%CI: 1.12–3.17, p = 0.017), AA genotype (OR: 1.95, 95%CI: 1.08– 3.53, p = 0.027), and A allele (OR: 1.44, 95%CI: 1.06–1.95, p = 0.019) were significantly associated with breast cancer risk. The results of meta-analysis showed a significant association between CCND1 c.870G>A polymorphism and breast cancer risk, especially in Caucasian population. In silico analysis revealed that c.870G>A transition affect CCND1 mRNA splicing and secondary structure.

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یونس آفتابیششم

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نام فایل تاریخ درج فایل اندازه فایل دانلود
Soleimani et al., 2016.pdf1396/04/211403743دانلود
2017-176.pdf1396/04/221343782دانلود